Determination of flutamide in tablets by high-performance liquid chromatography
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://www.latamjpharm.org/trabajos/24/2/LAJOP_24_2_3_1_48439399MF.pdf http://hdl.handle.net/11449/68197 |
Resumo: | Flutamide is a potent antiandrogen used for the treatment of prostatic cancer. A simple, sensitive and accurate high-performance liquid Chromatographic (HPLC) method is presented for quantitative determination of flutamide in tablets, using a reversed-phase technique and UV detection at 240 nm. The isocratic elution was used to quantify the analyte. The samples were chromatographed on Luna-C18 column and the mobile phase was 0.05 M phosphate buffer pH 4.0 - acetonitrile (50:50, v/v). The method was linear between 2.9 - 11.6 mg L -1. Over the tested concentration range the intra-day relative standard deviation for replicate analysis in tablets ranged from 0.44 to 0.78%. It was also found that the excipients in the commercial tablets did not interfere with the method. |
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Repositório Institucional da UNESP |
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Determination of flutamide in tablets by high-performance liquid chromatographyAnalysis in tabletsFlutamideHigh-performance liquid chromatography (HPLC)Pharmaceutical analysisacetonitrileflutamidedrug determinationhigh performance liquid chromatographyprostate cancerreversed phase high performance liquid chromatographytabletFlutamide is a potent antiandrogen used for the treatment of prostatic cancer. A simple, sensitive and accurate high-performance liquid Chromatographic (HPLC) method is presented for quantitative determination of flutamide in tablets, using a reversed-phase technique and UV detection at 240 nm. The isocratic elution was used to quantify the analyte. The samples were chromatographed on Luna-C18 column and the mobile phase was 0.05 M phosphate buffer pH 4.0 - acetonitrile (50:50, v/v). The method was linear between 2.9 - 11.6 mg L -1. Over the tested concentration range the intra-day relative standard deviation for replicate analysis in tablets ranged from 0.44 to 0.78%. It was also found that the excipients in the commercial tablets did not interfere with the method.Departamento de Fármacos e Medicamentos Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, Rod. Araraquara-Jaú, km 1, CEP 14801-902, Araraquara, SPPrograma de Pós-Graduação em Ciências Farmacêuticas FCF UNESPUniversidade Estadual Paulista, Baurú - SPDepartamento de Fármacos e Medicamentos Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista, Rod. Araraquara-Jaú, km 1, CEP 14801-902, Araraquara, SPPrograma de Pós-Graduação em Ciências Farmacêuticas FCF UNESPUniversidade Estadual Paulista, Baurú - SPUniversidade Estadual Paulista (Unesp)Salgado, Hérida Regina Nunes [UNESP]De Menezes, Manoel [UNESP]Storti, Madge Patrícia Betto [UNESP]2014-05-27T11:21:18Z2014-05-27T11:21:18Z2005-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article246-249http://www.latamjpharm.org/trabajos/24/2/LAJOP_24_2_3_1_48439399MF.pdfActa Farmaceutica Bonaerense, v. 24, n. 2, p. 246-249, 2005.0326-2383http://hdl.handle.net/11449/681972-s2.0-23044492305Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Farmaceutica Bonaerense0.4010,152info:eu-repo/semantics/openAccess2021-10-23T11:51:35Zoai:repositorio.unesp.br:11449/68197Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T11:51:35Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Determination of flutamide in tablets by high-performance liquid chromatography |
title |
Determination of flutamide in tablets by high-performance liquid chromatography |
spellingShingle |
Determination of flutamide in tablets by high-performance liquid chromatography Salgado, Hérida Regina Nunes [UNESP] Analysis in tablets Flutamide High-performance liquid chromatography (HPLC) Pharmaceutical analysis acetonitrile flutamide drug determination high performance liquid chromatography prostate cancer reversed phase high performance liquid chromatography tablet |
title_short |
Determination of flutamide in tablets by high-performance liquid chromatography |
title_full |
Determination of flutamide in tablets by high-performance liquid chromatography |
title_fullStr |
Determination of flutamide in tablets by high-performance liquid chromatography |
title_full_unstemmed |
Determination of flutamide in tablets by high-performance liquid chromatography |
title_sort |
Determination of flutamide in tablets by high-performance liquid chromatography |
author |
Salgado, Hérida Regina Nunes [UNESP] |
author_facet |
Salgado, Hérida Regina Nunes [UNESP] De Menezes, Manoel [UNESP] Storti, Madge Patrícia Betto [UNESP] |
author_role |
author |
author2 |
De Menezes, Manoel [UNESP] Storti, Madge Patrícia Betto [UNESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Salgado, Hérida Regina Nunes [UNESP] De Menezes, Manoel [UNESP] Storti, Madge Patrícia Betto [UNESP] |
dc.subject.por.fl_str_mv |
Analysis in tablets Flutamide High-performance liquid chromatography (HPLC) Pharmaceutical analysis acetonitrile flutamide drug determination high performance liquid chromatography prostate cancer reversed phase high performance liquid chromatography tablet |
topic |
Analysis in tablets Flutamide High-performance liquid chromatography (HPLC) Pharmaceutical analysis acetonitrile flutamide drug determination high performance liquid chromatography prostate cancer reversed phase high performance liquid chromatography tablet |
description |
Flutamide is a potent antiandrogen used for the treatment of prostatic cancer. A simple, sensitive and accurate high-performance liquid Chromatographic (HPLC) method is presented for quantitative determination of flutamide in tablets, using a reversed-phase technique and UV detection at 240 nm. The isocratic elution was used to quantify the analyte. The samples were chromatographed on Luna-C18 column and the mobile phase was 0.05 M phosphate buffer pH 4.0 - acetonitrile (50:50, v/v). The method was linear between 2.9 - 11.6 mg L -1. Over the tested concentration range the intra-day relative standard deviation for replicate analysis in tablets ranged from 0.44 to 0.78%. It was also found that the excipients in the commercial tablets did not interfere with the method. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-04-01 2014-05-27T11:21:18Z 2014-05-27T11:21:18Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://www.latamjpharm.org/trabajos/24/2/LAJOP_24_2_3_1_48439399MF.pdf Acta Farmaceutica Bonaerense, v. 24, n. 2, p. 246-249, 2005. 0326-2383 http://hdl.handle.net/11449/68197 2-s2.0-23044492305 |
url |
http://www.latamjpharm.org/trabajos/24/2/LAJOP_24_2_3_1_48439399MF.pdf http://hdl.handle.net/11449/68197 |
identifier_str_mv |
Acta Farmaceutica Bonaerense, v. 24, n. 2, p. 246-249, 2005. 0326-2383 2-s2.0-23044492305 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acta Farmaceutica Bonaerense 0.401 0,152 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
246-249 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1799965277488676864 |